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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received November 28, 2024
Accepted January 11, 2025
Available online June 25, 2025
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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The Role of Stack Pressure in Modulating Electrochemical Behavior of All-Solid-State Lithium–Sulfur Batteries

Department of Chemistry , Sungshin Women’s University , 55 Dobong-ro 76 ga-gil, Gangbuk-gu , Seoul 01133 , Republic of Korea 1School of Chemistry and Energy , Sungshin Women’s University , 55 Dobong-ro 76 ga-gil, Gangbuk-gu , Seoul 01133 , Republic of Korea 2Center for NanoBio Applied Technology , Sungshin Women’s University , 55 Dobong-ro 76 ga-gil, Gangbuk-gu , Seoul 01133 , Republic of Korea
Korean Journal of Chemical Engineering, June 2025, 42(7), 1507-1515(9)
https://doi.org/10.1007/s11814-025-00394-4

Abstract

All-solid-state lithium–sulfur batteries (ASSLSBs) represent a crucial frontier in energy storage research, promising higher

energy densities and improved safety over traditional lithium-ion systems. Despite their advantages, ASSLSBs face signifi -

cant challenges, particularly in addressing interfacial instability and mechanical issues arising from the insulating nature and

volume expansion of sulfur cathodes. Since the interfaces of all-solid-state batteries cannot accommodate the large volume

changes, interfacial contact issues become increasingly pronounced in systems utilizing S 8 conversion chemistry. Therefore,

applying stack pressure during cell operation is considered a critical factor for optimizing the performance and cycle life of

ASSLSB systems. In this study, we systematically investigated the impact of stack pressure on the electrochemical behavior

of ASSLSBs under four diff erent stack pressures. Electrochemical cycling results showed a marked diff erence in capacity

retention—74% retention after 100 cycles at high pressure, while only 6% capacity retention was observed at low pressure.

This pressure-dependent cycling performance was analyzed from two perspectives: the Li + /e

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